510(k) K881712 ยท DTB Permanent Pacemaker Electrode
MEDTRONIC MODEL 5866-36 LEAD ADAPTOR KIT
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, May 25, 1988 |
| Received | Apr 21, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881712
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.